Neural mechanisms for detecting and remembering novel events

Ranganath, Charan; Rainer, Gregor

doi:10.1038/nrn1052

Cited by 779Memory and Neural MechanismsNeural dynamics and brain functionNeuroscience and Neuropharmacology Research

Neural mechanisms for detecting and remembering novel events

Ranganath, Charan, Rainer, Gregor·2003·Nature Reviews Neuroscience

DOI 10.1038/nrn1052

Open this paper in CoChat — free account

Abstract

The ability to detect and respond to novel events is crucial for survival in a rapidly changing environment. Four decades of neuroscientific research has begun to delineate the neural mechanisms by which the brain detects and responds to novelty. Here, we review this research and suggest how changes in neural processing at the cellular, synaptic and network levels allow us to detect, attend to and subsequently remember the occurrence of a novel event.

Integrity signals

Registry

Crossref · 10.1038/nrn1052

Cites

142 of 142 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Sensory novelty, defined as a small number of stimulus exposures, enhances neural responses throughout visual, frontal and temporal areas.
“Sensory novelty, defined as a small number of stimulus exposures, is known to enhance neural responses throughout visual, frontal and temporal areas”
From Information-seeking, curiosity, and attention: computational and neural mechanisms (2013) · cites this paper as Ranganath and Rainer 2003
Sensory novelty activates reward-responsive dopamine-recipient areas.
“Sensory novelty, defined as a small number of stimulus exposures, is known to enhance neural responses throughout visual, frontal and temporal areas (Ranganath and Rainer 2003) and activate reward responsive dopamine-recipient areas.”
From Information-seeking, curiosity, and attention: computational and neural mechanisms (2013) · cites this paper as Ranganath and Rainer 2003

Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881 · see citing works
Neural Mechanisms of Selective Visual Attention
Desimone, R., & Duncan, J. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001205 · Cited by 8,388 · see citing works
Neurophysiological investigation of the basis of the fMRI signal
Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,542 · see citing works
Evoked-potential correlates of stimulus uncertainty
Sutton, S., Braren, M., Zubin, J., & John, E. R. (1965) · Science · doi:10.1126/science.150.3700.1187 · Cited by 3,061 · see citing works
Priming and Human Memory Systems
Tulving, E., & Schacter, D. L. (1990) · Science · doi:10.1126/science.2296719 · Cited by 2,595 · see citing works
Two varieties of long-latency positive waves evoked by unpredictable auditory stimuli in man
Squires, N. K., Squires, K. C., & Hillyard, S. A. (1975) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(75)90263-1 · Cited by 2,101 · see citing works
The Working Brain
Luria, A. R. (1973) · Cited by 1,861 · see citing works
Recognition memory: What are the roles of the perirhinal cortex and hippocampus?
Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,555 · see citing works
Neural Mechanisms of Visual Working Memory in Prefrontal Cortex of the Macaque
Miller, E. K., Erickson, C. A., & Desimone, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05154.1996 · Cited by 1,441 · see citing works
The novelty P3: an event-related brain potential (ERP) sign of the brain's evaluation of novelty
Friedman, D., Cycowicz, Y. M., & Gaeta, H. (2001) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00019-7 · Cited by 1,282 · see citing works
Interactive memory systems in the human brain
Poldrack, R. A., Clark, J., Paré-Blagoev, E. J., Shohamy, D., Creso Moyano, J., Myers, C., & Gluck, M. A. (2001) · Nature · doi:10.1038/35107080 · Cited by 1,132 · see citing works
fMR-adaptation: a tool for studying the functional properties of human cortical neurons
Kalanit Grill-spector, A., & Malach, R. (2001) · Acta Psychologica · doi:10.1016/s0001-6918(01)00019-1 · Cited by 1,068 · see citing works
Higher nervous functions: the orienting reflex
Sokolov, E. N. (1963) · Annual Review of Physiology · doi:10.1146/annurev.ph.25.030163.002553 · Cited by 1,026 · see citing works
Stimulus novelty, task relevance and the visual evoked potential in man
Courchesne, E., Hillyard, S. A., & Galambos, R. (1975) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(75)90003-6 · Cited by 1,012 · see citing works
The neural basis of the blood–oxygen–level–dependent functional magnetic resonance imaging signal
Logothetis, N. K. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1114 · Cited by 952 · see citing works
A multimodal cortical network for the detection of changes in the sensory environment
Downar, J., Crawley, A. P., Mikulis, D. J., & Davis, K. D. (2000) · Nature Neuroscience · doi:10.1038/72991 · Cited by 947 · see citing works
Practising orientation identification improves orientation coding in V1 neurons
Schoups, A., Vogels, R., Qian, N., & Orban, G. (2001) · Nature · doi:10.1038/35087601 · Cited by 856 · see citing works
Properties and mechanisms of perceptual priming
Wiggs, C. L., & Martin, A. D. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80144-x · Cited by 852 · see citing works
Contribution of human hippocampal region to novelty detection
Knight, R. T. (1996) · Nature · doi:10.1038/383256a0 · Cited by 834 · see citing works
Decreased response to novel stimuli after prefrontal lesions in man
Knight, R. T. (1984) · Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section · doi:10.1016/0168-5597(84)90016-9 · Cited by 828 · see citing works
Neuromodulation: acetylcholine and memory consolidation
Hasselmo, M. E. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01365-0 · Cited by 809 · see citing works
Endogenous Potentials Generated in the Human Hippocampal Formation and Amygdala by Infrequent Events
Halgren, E., Squires, N. K., Wilson, C. L., Rohrbaugh, J., Babb, T. L., & Crandall, P. H. (1980) · Science · doi:10.1126/science.7434000 · Cited by 778 · see citing works
The Neural Basis of Perceptual Learning
Gilbert, C. D., Sigman, M., & Crist, R. E. (2001) · Neuron · doi:10.1016/s0896-6273(01)00424-x · Cited by 688 · see citing works
Cortical Regions Involved in Perceiving Object Shape
Kourtzi, Z., & Kanwisher, N. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03310.2000 · Cited by 678 · see citing works
Über die Wirkung von Bereichsbildungen im Spurenfeld
von Restorff, H. (1933) · Psychological Research · doi:10.1007/bf02409636 · Cited by 643 · see citing works
Generators of the late cognitive potentials in auditory and visual oddball tasks
Halgren, E., Marinković, K., & Chauvel, P. (1998) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/s0013-4694(97)00119-3 · Cited by 641 · see citing works
Parallel Neuronal Mechanisms for Short-Term Memory
Miller, E. K., & Desimone, R. (1994) · Science · doi:10.1126/science.8290960 · Cited by 630 · see citing works
Functional-Anatomic Correlates of Object Priming in Humans Revealed by Rapid Presentation Event-Related fMRI
Buckner, R. L., Goodman, J. M., Burock, M. A., Rotte, M., Koutstaal, W., Schacter, D. L., Rosen, B. R., & Dale, A. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80456-0 · Cited by 622 · see citing works
On the neural generators of the P300 component of the event‐related potential
Johnson, R. (1993) · Psychophysiology · doi:10.1111/j.1469-8986.1993.tb03208.x · Cited by 612 · see citing works
Neural Activity in the Primate Prefrontal Cortex during Associative Learning
Asaad, W. F., Rainer, G., & Miller, E. K. (1998) · Neuron · doi:10.1016/s0896-6273(00)80658-3 · Cited by 593 · see citing works
Self-citation
Discharge of noradrenergic locus coeruleus neurons in behaving rats and monkeys suggests a role in vigilance
Aston‐Jones, G., Chiang, C., & Alexinsky, T. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63830-3 · Cited by 589 · see citing works
Novelty and Familiarity Activations in PET Studies of Memory Encoding and Retrieval
Tulving, E., Markowitsch, H. J., Craik, F. I. M., Habib, R., & Houle, S. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.1.71 · Cited by 558 · see citing works
The representation of stimulus familiarity in anterior inferior temporal cortex
Li, L., Miller, E. K., & Desimone, R. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.6.1918 · Cited by 539 · see citing works
Prefrontal–Temporal Circuitry for Episodic Encoding and Subsequent Memory
Kirchhoff, B. A., Wagner, A. D., Maril, A., & Stern, C. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06173.2000 · Cited by 536 · see citing works
Intracerebral potentials to rare target and distractor auditory and visual stimuli. III. Frontal cortex
Baudena, P., Halgren, E., Heit, G., & Clarke, J. M. (1995) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(95)98476-o · Cited by 530 · see citing works
Neuromodulatory transmitter systems in the cortex and their role in cortical plasticity
Gu, Q. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00026-x · Cited by 518 · see citing works
Intracerebral potentials to rare target and distractor auditory and visual stimuli. I. Superior temporal plane and parietal lobe
Halgren, E., Baudena, P., Clarke, J. M., Heit, G., Liégeois‐Chauvel, C., Chauvel, P., & Musolino, A. (1995) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(94)00259-n · Cited by 513 · see citing works
Contributions of temporal-parietal junction to the human auditory P3
Knight, R. T., Scabini, D., Woods, D. L., & Clayworth, C. C. (1989) · Brain Research · doi:10.1016/0006-8993(89)90466-6 · Cited by 506 · see citing works
Adaptation-Induced Plasticity of Orientation Tuning in Adult Visual Cortex
Dragoi, V., Sharma, J., & Sur, M. (2000) · Neuron · doi:10.1016/s0896-6273(00)00103-3 · Cited by 495 · see citing works
Pattern-selective adaptation in visual cortical neurones
Movshon, J. A., & Lennie, P. (1979) · Nature · doi:10.1038/278850a0 · Cited by 465 · see citing works
Rapid Adaptation in Visual Cortex to the Structure of Images
Müller, J. R., Metha, A. B., Krauskopf, J., & Lennie, P. (1999) · Science · doi:10.1126/science.285.5432.1405 · Cited by 458 · see citing works
Neural response suppression, haemodynamic repetition effects, and behavioural priming
Henson, R. N., & Rugg, M. D. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00159-8 · Cited by 444 · see citing works
Noradrenergic innervation of the adult rat hippocampal formation
Loy, R., Koziell, D. A., Lindsey, J. D., & Moore, R. Y. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901890406 · Cited by 443 · see citing works
Intracerebral potentials to rare target and distractor auditory and visual stimuli. II. Medial, lateral and posterior temporal lobe
Halgren, E., Baudena, P., Clarke, J. M., Heit, G., Marinkovic, K., Devaux, B., Vignal, J.-P., & Biraben, A. (1995) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(95)98475-n · Cited by 432 · see citing works
Prospective coding for objects in primate prefrontal cortex
Rainer, G., Rao, S. C., & Miller, E. K. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05493.1999 · Cited by 432 · see citing works
Self-citation
Neural Origins of the P300
Soltani, M., & Knight, R. T. (2000) · Critical Reviews in Neurobiology · doi:10.1615/critrevneurobiol.v14.i3-4.20 · Cited by 423 · see citing works
P300 and Recall in an Incidental Memory Paradigm
Fabiani, M., Karis, D., & Donchin, E. (1986) · Psychophysiology · doi:10.1111/j.1469-8986.1986.tb00636.x · Cited by 411 · see citing works
Amygdala–Hippocampal Involvement in Human Aversive Trace Conditioning Revealed through Event-Related Functional Magnetic Resonance Imaging
Büchel, C., Dolan, R. J., Armony, J. L., & Friston, K. J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-24-10869.1999 · Cited by 404 · see citing works
Neural sources involved in auditory target detection and novelty processing: An event-related fMRI study
Kiehl, K. A., Laurens, K. R., Duty, T., Forster, B. B., & Liddle, P. F. (2001) · Psychophysiology · doi:10.1111/1469-8986.3810133 · Cited by 397 · see citing works
Noradrenergic and serotoninergic innervation of cortical, thalamic, and tectal visual structures in old and new world monkeys
Morrison, J. H., & Foote, S. L. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902430110 · Cited by 392 · see citing works
Medial Temporal Lobe Activity Associated with Active Maintenance of Novel Information
Charan Ranganath, A., & D’Esposito, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00411-1 · Cited by 391 · see citing works
Language-related field potentials in the anterior-medial temporal lobe: II. Effects of word type and semantic priming
Nobre, A. C., & McCarthy, G. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-02-01090.1995 · Cited by 383 · see citing works
Neuronal activity related to visual recognition memory: long-term memory and the encoding of recency and familiarity information in the primate anterior and medial inferior temporal and rhinal cortex
Fahy, F. L., Riches, I. P., & Brown, M. W. (1993) · Experimental Brain Research · doi:10.1007/bf00234113 · Cited by 359 · see citing works
Language-related field potentials in the anterior-medial temporal lobe: I. Intracranial distribution and neural generators
McCarthy, G., Nobre, A. C., Shlomo Bentin, A., & Spencer, D. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-02-01080.1995 · Cited by 356 · see citing works
Responses of neurons in the inferior temporal cortex in short term and serial recognition memory tasks
Baylis, G. C., & Rolls, E. T. (1987) · Experimental Brain Research · doi:10.1007/bf00235984 · Cited by 351 · see citing works
Stimulus context determines P3a and P3b
Katayama, J., & Polich, J. M. (1998) · Psychophysiology · doi:10.1111/1469-8986.3510023 · Cited by 346 · see citing works
Neural Correlate of Perceptual Adaptation to Gratings
Maffei, L., Fiorentini, A., & Bisti, S. (1973) · Science · doi:10.1126/science.182.4116.1036 · Cited by 338 · see citing works
The effects of visual stimulation and memory on neurons of the hippocampal formation and the neighboring parahippocampal gyrus and inferior temporal cortex of the primate
Riches, I. P., Wilson, F., & Mw, B. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-06-01763.1991 · Cited by 336 · see citing works
Segregating the functions of human hippocampus
Strange, B. A., Fletcher, P. C., Henson, R. N., Friston, K. J., & Dolan, R. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.4034 · Cited by 332 · see citing works
Recognition memory: neuronal substrates of the judgement of prior occurrence
Brown, M. W., & Xiang, J. ‐. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00002-1 · Cited by 329 · see citing works
Cellular Mechanisms of Long-Lasting Adaptation in Visual Cortical Neurons In Vitro
Sanchez-Vives, M. V., Nowak, L. G., & McCormick, D. A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04286.2000 · Cited by 320 · see citing works
NEURAL INPUTS INTO THE NUCLEUS BASALIS OF THE SUBSTANTIA INNOMINATA (Ch4) IN THE RHESUS MONKEY
Mesulam, M. M., & Mufson, E. J. (1984) · Brain · doi:10.1093/brain/107.1.253 · Cited by 316 · see citing works
Physiological Correlates of Perceptual Learning in Monkey V1 and V2
Ghose, G. M., Yang, T., & Maunsell, J. H. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00690.2001 · Cited by 310 · see citing works
Response to Novelty and its Rapid Habituation in Locus Coeruleus Neurons of the Freely Exploring Rat
Vankov, A., Hervé‐Minvielle, A., & Sara, S. J. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01108.x · Cited by 309 · see citing works
Anatomic Bases of Event-Related Potentials and Their Relationship to Novelty Detection in Humans
Knight, R. T., & Scabini, D. (1998) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-199801000-00003 · Cited by 298 · see citing works
Perceiving patterns in random series: dynamic processing of sequence in prefrontal cortex
Huettel, S. A., Mack, P. B., & McCarthy, G. (2002) · Nature Neuroscience · doi:10.1038/nn841 · Cited by 297 · see citing works
Responses to Rare Visual Target and Distractor Stimuli Using Event-Related fMRI
Clark, V. P., Fannon, S. P., Lai, S., Benson, R. R., & Bauer, L. O. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.3133 · Cited by 295 · see citing works
Neuronal Basis of the Motion Aftereffect Reconsidered
Huk, A. C., Ress, D. B., & Heeger, D. J. (2001) · Neuron · doi:10.1016/s0896-6273(01)00452-4 · Cited by 293 · see citing works
Effects of Visual Experience on the Representation of Objects in the Prefrontal Cortex
Rainer, G., & Miller, E. K. (2000) · Neuron · doi:10.1016/s0896-6273(00)00019-2 · Cited by 285 · see citing works
Self-citation
Review of the historical, empirical, and theoretical status of the von Restorff phenomenon.
Wallace, W. P. (1965) · Psychological Bulletin · doi:10.1037/h0022001 · Cited by 273 · see citing works
The subtlety of distinctiveness: What von Restorff really did
Hunt, R. R. (1995) · Psychonomic Bulletin & Review · doi:10.3758/bf03214414 · Cited by 270 · see citing works
Effects of novelty and habituation on acetylcholine, GABA, and glutamate release from the frontal cortex and hippocampus of freely moving rats
Giovannini, M. G., Rakovska, A., Benton, R. S., Pazzagli, M., Bianchi, L., & Pepeu, G. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00266-4 · Cited by 267 · see citing works
The central role of the prefrontal cortex in directing attention to novel events
Daffner, K. R., Mesulam, M. M., Scinto, L. F. M., Acar, D., Calvo, V., Faust, R. R., Chabrerie, A. V., Kennedy, B., & Holcomb, P. J. (2000) · Brain · doi:10.1093/brain/123.5.927 · Cited by 265 · see citing works
Task-dependent field potentials in human hippocampal formation
McCarthy, G., Wood, C. C., Williamson, P., & Spencer, D. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-12-04253.1989 · Cited by 265 · see citing works
Left Anterior Prefrontal Activation Increases with Demands to Recall Specific Perceptual Information
Ranganath, C., Johnson, M. K., & D’Esposito, M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-j0005.2000 · Cited by 256 · see citing works
Self-citation
Distributed Cortical Network for Visual Attention
Knight, R. T. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.1.75 · Cited by 255 · see citing works
Anterior and posterior association cortex contributions to the somatosensory P300
Yamaguchi, S., & Knight, R. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-07-02039.1991 · Cited by 254 · see citing works
Effects of mnemonic strategy manipulation in a Von Restorff paradigm
Fabiani, M., Karis, D., & Donchin, E. (1990) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(90)90149-e · Cited by 253 · see citing works
Prefrontal activation evoked by infrequent target and novel stimuli in a visual target detection task: An event-related functional magnetic resonance imaging study
Kirino, E., Belger, A., Goldman-Rakic, P., & McCarthy, G. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06612.2000 · Cited by 226 · see citing works
The effect of learning on the face selective responses of neurons in the cortex in the superior temporal sulcus of the monkey
Rolls, E. T., Baylis, G. C., Hasselmo, M. E., & Nalwa, V. (1989) · Experimental Brain Research · doi:10.1007/bf00253632 · Cited by 223 · see citing works
Functional MRI detection of pharmacologically induced memory impairment
Sperling, R. A., Greve, D. N., Dale, A. M., Killiany, R., Holmes, J., Rosas, H. D., Cocchiarella, A. J., Firth, P. G., Rosen, B. R., Lake, S. L., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.012467899 · Cited by 210 · see citing works
Neurochemical Substrates and Neuroanatomical Generators of the Event-Related P300
Frodl, T., Ronald Bottlender, A., & Hegerl, U. (1999) · Neuropsychobiology · doi:10.1159/000026603 · Cited by 205 · see citing works
Encoding processes and memory organization: A model of the von Restorff effect.
Fabiani, M., & Donchin, E. (1995) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.21.1.224 · Cited by 201 · see citing works
The functional neuroanatomy of novelty processing: integrating ERP and fMRI results
Opitz, B. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.4.379 · Cited by 195 · see citing works
ERP amplitude and scalp distribution to target and novel events: effects of temporal order in young, middle-aged and older adults
Friedman, D. S., & Simpson, G. V. (1994) · Cognitive Brain Research · doi:10.1016/0926-6410(94)90020-5 · Cited by 183 · see citing works
Electrophysiological evidence for the involvement of the locus coeruleus in alerting, orienting, and attending
Foote, S. L., Berridge, C. W., Adams, L. M., & Pineda, J. A. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63831-5 · Cited by 181 · see citing works
On the relationship of P3a and the Novelty-P3
Simons, R. F., Graham, F. K., Miles, M. A., & Chen, X. (2001) · Biological Psychology · doi:10.1016/s0301-0511(01)00078-3 · Cited by 171 · see citing works
Stimulus specific adaptation in inferior temporal and medial temporal cortex of the monkey
Ringo, J. L. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00197-2 · Cited by 169 · see citing works
Human temporal lobe potentials in verbal learning and memory processes
Elger, C. E., Grünwald, T., Lehnertz, K., Marta Kutas, A., Helmstaedter, C., Brockhaus, A., Roost, D. V., & Heinze, H. J. (1997) · Neuropsychologia · doi:10.1016/s0028-3932(96)00110-8 · Cited by 164 · see citing works
Neuronal responses related to the novelty and familiarity of visual stimuli in the substantia innominata, diagonal band of Broca and periventricular region of the primate basal forebrain
Wilson, F. A. W., & Rolls, E. T. (1990) · Experimental Brain Research · doi:10.1007/bf00228852 · Cited by 164 · see citing works
Orbitofrontal cortex and dynamic filtering of emotional stimuli
Rule, R. R., Shimamura, A. P., & KNIGHT, R. T. (2002) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.2.3.264 · Cited by 163 · see citing works
Supplementary eye field contrasted with the frontal eye field during acquisition of conditional oculomotor associations
Chen, L. L., & Wise, S. P. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.3.1122 · Cited by 161 · see citing works
Habituation-like decrease in the responses of neurons in inferior temporal cortex of the macaque
Miller, E. K., Gochin, P. M., & Gross, C. G. (1991) · Visual Neuroscience · doi:10.1017/s0952523800004843 · Cited by 160 · see citing works
Verbal novelty detection within the human hippocampus proper
Grünwald, T., Lehnertz, K., Heinze, H. J., Helmstaedter, C., & Elger, C. E. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3193 · Cited by 160 · see citing works
P3a, perceptual distinctiveness, and stimulus modality
Comerchero, M. D., & Polich, J. M. (1998) · Cognitive Brain Research · doi:10.1016/s0926-6410(98)00009-3 · Cited by 157 · see citing works
Wavelet Analysis of P3a and P3b
Demıralp, T., Ademoğlu, A., Comerchero, M. D., & Polich, J. M. (2001) · Brain Topography · doi:10.1023/a:1011102628306 · Cited by 156 · see citing works
Evidence relating human verbal memory to hippocampal N -methyl- d- aspartate receptors
Grünwald, T., Beck, H., Lehnertz, K., Blümcke, I., Pezer, N., Kurthen, M., Fernández, G., Roost, D. V., Heinze, H. J., Marta Kutas, A., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12085 · Cited by 142 · see citing works
Learning impairments following injection of a selective cholinergic immunotoxin, ME20.4 IgG-saporin, into the basal nucleus of Meynert in monkeys
Fine, A., Hoyle, C., Maclean, C. J., LeVatte, T. L., Baker, H. F., & Ridley, R. M. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00208-x · Cited by 138 · see citing works
Systematic regional differences in the cholinergic innervation of the primate cerebral cortex: Distribution of enzyme activities and some behavioral implications
Mesulam, M. M., Volicer, L., Marquis, J. K., Mufson, E. J., & Green, R. C. (1986) · Annals of Neurology · doi:10.1002/ana.410190206 · Cited by 135 · see citing works
Noradrenergic innervation of monkey prefrontal cortex: A dopamine‐β‐hydroxylase immunohistochemical study
Lewis, D. A., & Morrison, J. H. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902820302 · Cited by 131 · see citing works
A Review of EEG and Blood Flow Data
Knight, R. T., & Nakada, T. (1998) · Reviews in the Neurosciences · doi:10.1515/revneuro.1998.9.1.57 · Cited by 129 · see citing works
Multiple Sources of P3b Associated with Different Types of Information
Ruchkin, D. S., Johnson, R., Canoune, H. L., et al. (1990) · Psychophysiology · doi:10.1111/j.1469-8986.1990.tb00367.x · Cited by 129 · see citing works
Effects of aging on the novelty P3 during attend and ignore oddball tasks
Friedman, D., Kazmerski, V. A., & Cycowicz, Y. M. (1998) · Psychophysiology · doi:10.1017/s0048577298970664 · Cited by 124 · see citing works
Learning and memory is reflected in the responses of reinforcement- related neurons in the primate basal forebrain
Wilson, F., & Rolls, E. T. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01254.1990 · Cited by 120 · see citing works
Motion Processing in the Macaque: Revisited with Functional Magnetic Resonance Imaging
Tolias, A. S., Smirnakis, S. M., Augath, M. A., Trinath, T., & Logothetis, N. K. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08594.2001 · Cited by 117 · see citing works
Adaptive anterior hippocampal responses to oddball stimuli
Strange, B. A., & Dolan, R. J. (2001) · Hippocampus · doi:10.1002/hipo.1084 · Cited by 117 · see citing works
Timecourse of object‐related neural activity in the primate prefrontal cortex during a short‐term memory task
Rainer, G., & Miller, E. K. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.01958.x · Cited by 113 · see citing works
Self-citation
An Event-Related fMRI Study of Visual and Auditory Oddball Tasks
Kiehl, K. A., Laurens, K. R., Duty, T., Forster, B. B., & Liddle, P. F. (2001) · Journal of Psychophysiology · doi:10.1027//0269-8803.15.4.221 · Cited by 113 · see citing works
Repetition priming of words, pseudowords, and nonwords.
Stark, C. E. L., & McClelland, J. L. (2000) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.26.4.945 · Cited by 109 · see citing works
Short-and Long-Delay Intracranial ERP Repetition Effects Dissociate Memory Systems in the Human Brain
Guillem, F., Rougier, A., & Claverie, B. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563526 · Cited by 100 · see citing works
Regulation of attention to novel stimuli by frontal lobes
Daffner, K. R., Mesulam, M. M., Scinto, L. F. M., Cohen, L. G., Kennedy, B. P., West, W. C., & Holcomb, P. J. (1998) · Neuroreport · doi:10.1097/00001756-199803300-00004 · Cited by 98 · see citing works
Pharmacological Modulation of Behavioral and Neuronal Correlates of Repetition Priming
Thiel, C. M., Henson, R. N., Morris, J. S., Friston, K. J., & Dolan, R. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06846.2001 · Cited by 97 · see citing works
Reproducibility of the hemodynamic response to auditory oddball stimuli: A six‐week test–retest study
Kiehl, K. A., & Liddle, P. F. (2002) · Human Brain Mapping · doi:10.1002/hbm.10074 · Cited by 97 · see citing works
Effect of Sound Familiarity on the Event-Related Potentials Elicited by Novel Environmental Sounds
Cycowicz, Y. M., & Friedman, D. (1998) · Brain and Cognition · doi:10.1006/brcg.1997.0955 · Cited by 94 · see citing works
Integrated brain activity in medial temporal and prefrontal areas predicts subsequent memory performance: human declarative memory formation at the system level
Fernández, G., & Tendolkar, I. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00494-4 · Cited by 92 · see citing works
Memory encoding and hippocampally-based novelty/familiarity discrimination networks
Habib, R., McIntosh, A. R., Wheeler, M. A., & Tulving, E. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00160-4 · Cited by 86 · see citing works
The von Restorff Effect in Visual Object Recognition Memory in Humans and Monkeys: The Role of Frontal/Perirhinal Interaction
Parker, A. J., Wilding, E. L., & Akerman, C. J. (1998) · Journal of Cognitive Neuroscience · doi:10.1162/089892998563103 · Cited by 83 · see citing works
Intracranial recordings of endogenous ERPs in humans
McCarthy, G. (1985) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(85)90083-5 · Cited by 82 · see citing works
Disruption of attention to novel events after frontal lobe injury in humans
Daffner, K. R. (2000) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.68.1.18 · Cited by 79 · see citing works
Chapter 3: Catecholaminergic-cholinergic interaction in the basal forebrain
Záborszky, L., Cullinan, W. E., & Luine, V. N. (1993) · Progress in brain research · doi:10.1016/s0079-6123(08)62379-1 · Cited by 77 · see citing works
Stimulus specific adaptation in excited but not in inhibited cells in inferotemporal cortex of Macaque
Sobótka, S., & Ringo, J. L. (1994) · Brain Research · doi:10.1016/0006-8993(94)90061-2 · Cited by 76 · see citing works
P3a from a passive visual stimulus task
Jeon, Y., & Polich, J. M. (2001) · Clinical Neurophysiology · doi:10.1016/s1388-2457(01)00663-0 · Cited by 75 · see citing works
The orienting reflex
Olst, E. H. (1971) · De Gruyter eBooks · doi:10.1515/9783111557052 · Cited by 73 · see citing works
Adaptation to contingencies in macaque primary visual cortex
Carandini, M., Barlow, H. B., O’Keefe, L. P., et al. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0098 · Cited by 71 · see citing works
Alterations of intrahippocampal cognitive potentials in temporal lobe epilepsy
Grünwald, T., Elger, C. E., Lehnertz, K., Roost, D. V., & Heinze, H. J. (1995) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(95)00015-q · Cited by 70 · see citing works
Repetition priming of words, pseudowords, and nonwords.
Stark, C. E. L., & McClelland, J. L. (2000) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.26.4.945 · Cited by 68 · see citing works
Scopolamine affects short-term memory but not inferior temporal neurons
Miller, E. K., & Desimone, R. (1993) · NeuroReport · doi:10.1097/00001756-199301000-00021 · Cited by 66 · see citing works
Scopolamine but Not Lorazepam Modulates Face Repetition Priming A Psychopharmacological fMRI Study
Thiel, C. M. (2002) · Neuropsychopharmacology · doi:10.1016/s0893-133x(02)00316-0 · Cited by 66 · see citing works
Human intracerebral potentials associated with target, novel, and omitted auditory stimuli
Alain, C., Richer, F., Achim, A., et al. (1989) · Brain Topography · doi:10.1007/bf01129601 · Cited by 64 · see citing works
Limbic P300s in temporal lobe epilepsy with and without Ammon's horn sclerosis
Grünwald, T., Beck, H., Lehnertz, K., et al. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00613.x · Cited by 63 · see citing works
A model for experience-dependent changes in the responses of inferotemporal neurons
Sohal, V. S., & Hasselmo, M. E. (2000) · Network Computation in Neural Systems · doi:10.1088/0954-898x_11_3_301 · Cited by 60 · see citing works
Intracranial ERPs in humans during a lateralized visual oddball task: II. Temporal, parietal, and frontal recordings
Clarke, J. M., Halgren, E., & Chauvel, P. (1999) · Clinical Neurophysiology · doi:10.1016/s1388-2457(99)00064-4 · Cited by 56 · see citing works
Scopolamine impairs memory performance and reduces frontal but not parietal visual P3 amplitude
Potter, D. D., Pickles, C., ROBERTS, R. C., et al. (2000) · Biological Psychology · doi:10.1016/s0301-0511(99)00023-x · Cited by 46 · see citing works
Crossed unilateral lesions of the medial forebrain bundle and either inferior temporal or frontal cortex impair object–reward association learning in Rhesus monkeys
Easton, A., & Gaffan, D. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00098-1 · Cited by 40 · see citing works
Frontal Brain Activity during Episodic and Semantic Retrieval: Insights from Event-Related Potentials
Charan Ranganath, A., & Paller, K. A. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563661 · Cited by 38 · see citing works
On the relation between conceptual priming, neural priming, and novelty assessment
Habib, R. (2001) · Scandinavian Journal of Psychology · doi:10.1111/1467-9450.00230 · Cited by 37 · see citing works
Repetition of novel stimuli in an ERP oddball paradigm: Aging effects
Kazmerski, V. A., & Friedman, D. (1995) · Journal of Psychophysiology · Cited by 36 · see citing works
Crossed unilateral lesions of medial forebrain bundle and either inferior temporal or frontal cortex impair object recognition memory in Rhesus monkeys
Easton, A., Parker, A. J., & Gaffan, D. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00384-3 · Cited by 30 · see citing works
Intracranial ERPs in humans during a lateralized visual oddball task: I. Occipital and peri-Rolandic recordings
Clarke, J. M., Halgren, E., & Chauvel, P. (1999) · Clinical Neurophysiology · doi:10.1016/s1388-2457(99)00063-2 · Cited by 24 · see citing works
Monkey P3 in an “oddball” paradigm: Pharmacological support for multiple neural sources
Pineda, J. A., & Westerfield, M. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90142-x · Cited by 21 · see citing works
The Effect of Cholinergic Receptor Blockade by Scopolamine on Memory Performance and the Auditory P3
Potter, D. D., Pickles, C., ROBERTS, R. C., et al. (2000) · Journal of Psychophysiology · doi:10.1027//0269-8803.14.1.11 · Cited by 15 · see citing works
The Neural Substrates of Cognitive Event-Related Potentials: A Review of Animal Models of P3
Paller, K. A. (1994) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4612-0283-7_14 · Cited by 15 · see citing works

Flagged first, then by citations

Sorted by citations

Updating P300: An integrative theory of P3a and P3b
Polich, J. (2007) · Clinical Neurophysiology · doi:10.1016/j.clinph.2007.04.019 · Cited by 7,919 · see citing works
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · see citing works
“5), novelty checking is not a new, unique, emotion-specific mental operation – there are many studies on novelty processing in cognitive (see Ranganath & Rainer 2003) and affective neuroscience (Balderston et al. 2011).”
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738 · see citing works
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377 · see citing works
Self-citation
Bayesian surprise attracts human attention
Itti, L., & Baldi, P. (2009) · Vision Research · doi:10.1016/j.visres.2008.09.007 · Cited by 1,224 · see citing works
Discovering Event Structure in Continuous Narrative Perception and Memory
Baldassano, C., Chen, J., Zadbood, A., Pillow, J. W., Hasson, U., & Norman, K. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.041 · Cited by 952 · see citing works
Vigilance, alertness, or sustained attention: physiological basis and measurement
Oken, B. S., Salinsky, M. C., & Elsas, S. M. (2006) · Clinical Neurophysiology · doi:10.1016/j.clinph.2006.01.017 · Cited by 887 · see citing works
Information-seeking, curiosity, and attention: computational and neural mechanisms
Gottlieb, J., Oudeyer, P.-Y., Lopes, M., & Baranes, A. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.001 · Cited by 784 · see citing works
“Sensory novelty, defined as a small number of stimulus exposures, is known to enhance neural responses throughout visual, frontal and temporal areas (Ranganath and Rainer 2003) and activate reward responsive dopamine-recipient areas.”
Reward-related FMRI activation of dopaminergic midbrain is associated with enhanced hippocampus-dependent long-term memory formation
Wittmann, B. C., Schott, B. H., Guderian, S., Frey, J. U., Heinze, H.-J., & Düzel, E. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.010 · Cited by 698 · see citing works
Dissociable correlates of recollection and familiarity within the medial temporal lobes
Ranganath, C., Yonelinas, A. P., Cohen, M. X., Dy, C. J., Tom, S. M., & D’Esposito, M. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2003.07.006 · Cited by 689 · see citing works
Self-citation
A direct brainstem–amygdala–cortical ‘alarm’system for subliminal signals of fear.
Liddell, B. J., Brown, K. J., Kemp, A. H., Barton, M. J., Das, P., Peduto, A., Gordon, E., & Williams, L. M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.08.016 · Cited by 670 · see citing works
Recollection and familiarity: Examining controversial assumptions and new directions
Yonelinas, A. P., Aly, M., Wang, W., & Koen, J. D. (2010) · Hippocampus · doi:10.1002/hipo.20864 · Cited by 571 · see citing works
“In addition to perception and short-term memory, the MTL also appears to play a role in the processing and detection of novelty (for reviews, see Ranganath and Rainer, 2003; Nyberg, 2005; Kumaran and Maguire, 2007, 2009).”
Background
The hierarchical basis of neurovisceral integration
Smith, R., Thayer, J. F., Khalsa, S. S., & Lane, R. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.003 · Cited by 523 · see citing works
The origin of mind: Evolution of brain, cognition, and general intelligence.
Geary, D. C. (2005) · doi:10.1037/10871-000 · Cited by 551 · see citing works
Novelty or Surprise?
Barto, A., Mirolli, M., & Baldassarre, G. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00907 · Cited by 397 · see citing works
Effects of Healthy Aging on Hippocampal and Rhinal Memory Functions: An Event-Related fMRI Study
Daselaar, S. M., Fleck, M. S., Dobbins, I. G., Madden, D. J., & Cabeza, R. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj112 · Cited by 392 · see citing works
A unified framework for the functional organization of the medial temporal lobes and the phenomenology of episodic memory
Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375 · see citing works
Self-citation
Nociceptive Laser-Evoked Brain Potentials Do Not Reflect Nociceptive-Specific Neural Activity
Mouraux, A., & Iannetti, G. D. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91181.2008 · Cited by 373 · see citing works
Statistical learning of visual transitions in monkey inferotemporal cortex
Meyer, T., & Olson, C. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112895108 · Cited by 325 · see citing works
Amygdala–prefrontal dissociation of subliminal and supraliminal fear
Williams, L. M., Liddell, B. J., Kemp, A. H., Bryant, R. A., Meares, R. A., Peduto, A. S., & Gordon, E. (2006) · Human Brain Mapping · doi:10.1002/hbm.20208 · Cited by 257 · see citing works
Mechanisms underlying working memory for novel information
Hasselmo, M. E., & Stern, C. E. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.09.005 · Cited by 249 · see citing works
The consolidation of object and context recognition memory involve different regions of the temporal lobe
Balderas, I., Rodriguez-Ortiz, C. J., Salgado-Tonda, P., Chavez-Hurtado, J., McGaugh, J. L., & Bermudez-Rattoni, F. (2008) · Learning & Memory · doi:10.1101/lm.1028008 · Cited by 213 · see citing works
Hippocampal contributions to the episodic simulation of specific and general future events
Addis, D. R., Cheng, T., P. Roberts, R., & Schacter, D. L. (2011) · Hippocampus · doi:10.1002/hipo.20870 · Cited by 182 · see citing works
The nucleus accumbens as a nexus between values and goals in goal-directed behavior: a review and a new hypothesis
Mannella, F., Gurney, K., & Baldassarre, G. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00135 · Cited by 166 · see citing works
Novelty, conditioning and attentional bias to sexual rewards
Banca, P., Morris, L. S., Mitchell, S., Harrison, N. A., Potenza, M. N., & Voon, V. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2015.10.017 · Cited by 137 · see citing works
Novelty increases the mesolimbic functional connectivity of the substantia nigra/ventral tegmental area (SN/VTA) during reward anticipation: Evidence from high-resolution fMRI
Krebs, R. M., Heipertz, D., Schuetze, H., & Duzel, E. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.06.038 · Cited by 135 · see citing works
Brain training in progress: a review of trainability in healthy seniors
Buitenweg, J. I. V., Murre, J. M. J., & Ridderinkhof, K. R. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00183 · Cited by 132 · see citing works
Personality traits are differentially associated with patterns of reward and novelty processing in the human substantia nigra/ventral tegmental area
Krebs, R. M., Schott, B. H., & Düzel, E. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.08.019 · Cited by 129 · see citing works
Culture and Context: East Asian American and European American Differences in P3 Event-Related Potentials and Self-Construal
Lewis, R. S., Goto, S. G., & Kong, L. L. (2008) · Personality and Social Psychology Bulletin · doi:10.1177/0146167207313731 · Cited by 118 · see citing works
Catecholaminergic Regulation of Learning Rate in a Dynamic Environment
Jepma, M., Murphy, P. R., Nassar, M. R., Rangel-Gomez, M., Meeter, M., & Nieuwenhuis, S. (2016) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005171 · Cited by 91 · see citing works
Brain reactivity differentiates subjects with high and low dream recall frequencies during both sleep and wakefulness
Eichenlaub, J.-B., Bertrand, O., Morlet, D., & Ruby, P. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs388 · Cited by 101 · see citing works
The P300 event-related brain potential as a neurobiological endophenotype for substance use disorders: a meta-analytic investigation
Euser, A. S., Arends, L. R., Evans, B. E., Greaves-Lord, K., Huizink, A. C., & Franken, I. H. A. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.09.002 · Cited by 100 · see citing works
The representation of prediction error in auditory cortex
Rubin, J., Ulanovsky, N., Nelken, I., & Tishby, N. (2016) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005058 · Cited by 87 · see citing works
The Role of the Lateral Frontal Cortex in Causal Associative Learning: Exploring Preventative and Super-learning
Turner, D. C. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh046 · Cited by 94 · see citing works
Novel scenes improve recollection and recall of words
Fenker, D. B., Frey, J. U., Schuetze, H., Heipertz, D., Heinze, H.-J., & Duzel, E. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20086 · Cited by 94 · see citing works
Effects of Inflammation on Hippocampus and Substantia Nigra Responses to Novelty in Healthy Human Participants
Harrison, N. A., Cercignani, M., Voon, V., & Critchley, H. D. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.222 · Cited by 89 · see citing works
Auditory and visual cortical activity during selective attention in fragile X syndrome: a cascade of processing deficiencies.
Van der Molen, M. J. W., Van der Molen, M. W., Ridderinkhof, K. R., Hamel, B. C. J., Curfs, L. M. G., & Ramakers, G. J. A. (2012) · Clinical Neurophysiology · doi:10.1016/j.clinph.2011.08.023 · Cited by 88 · see citing works
Dynamics of Memory Representations in Networks with Novelty-Facilitated Synaptic Plasticity
Blumenfeld, B., Preminger, S., Sagi, D., & Tsodyks, M. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.016 · Cited by 79 · see citing works
Intrinsic motivations and open-ended development in animals, humans, and robots: an overview
Baldassarre, G., Stafford, T., Mirolli, M., Redgrave, P., Ryan, R. M., & Barto, A. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00985 · Cited by 73 · see citing works
Balancing new against old information: the role of puzzlement surprise in learning
Faraji, M., Preuschoff, K., & Gerstner, W. (2018) · Neural Computation · doi:10.1162/neco_a_01025 · Cited by 68 · see citing works
Neural correlates of the spacing effect in explicit verbal semantic encoding support the deficient‐processing theory
Callan, D. E., & Schweighofer, N. (2010) · Human Brain Mapping · doi:10.1002/hbm.20894 · Cited by 55 · see citing works
Learning probabilistic neural representations with randomly connected circuits
Maoz, O., Tkačik, G., Esteki, M. S., Kiani, R., & Schneidman, E. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912804117 · Cited by 44 · see citing works
Expectation and temperament moderate amygdala and dorsal anterior cingulate cortex responses to fear faces
Clauss, J. A., Cowan, R. L., & Blackford, J. U. (2011) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-010-0007-9 · Cited by 34 · see citing works
Apolipoprotein E ε4-related thickening of the cerebral cortex modulates selective attention
Espeseth, T., Westlye, L. T., Walhovd, K. B., Fjell, A. M., Endestad, T., Rootwelt, H., & Reinvang, I. (2012) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.12.027 · Cited by 32 · see citing works
Distractibility in AD/HD predominantly inattentive and combined subtypes: the P3a ERP component, heart rate and performance
KEAGE, H. A. D., CLARK, C. R., HERMENS, D. F., KOHN, M. R., CLARKE, S., WILLIAMS, L. M., CREWTHER, D., LAMB, C., & GORDON, E. (2006) · Journal of Integrative Neuroscience · doi:10.1142/s0219635206001070 · Cited by 30 · see citing works
Auditory novelty processing is enhanced in obsessive–compulsive disorder
Ischebeck, M., Endrass, T., Simon, D., & Kathmann, N. (2011) · Depression and Anxiety · doi:10.1002/da.20886 · Cited by 27 · see citing works

Authors: Ranganath, C., & Rainer, G.
Affiliations: Max Planck Society (DE)
ORCID: Rainer, Gregor
Venue: Nature Reviews Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2003-03
Volume: 4
Issue: 3
Pages: 193-202
ISSN: 1471-003X (ISSN-L)
1471-0048
DOI: 10.1038/nrn1052
OpenAlex: W1998127479
Cited by: 779
References: 142
Citations by year: 2026: 25 · 2025: 39 · 2024: 33 · 2023: 22 · 2022: 39 · 2021: 46 · 2020: 39 · 2019: 33 · 2018: 33 · 2017: 28 · 2016: 42 · 2015: 45 · 2014: 42 · 2013: 31 · 2012: 37
FWCI: 3.13
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature reviews. Neuroscience (publishedVersion)
PubMed (publishedVersion)
Max Planck Institute for Plasma Physics (submittedVersion)
MPG.PuRe (Max Planck Society) (submittedVersion)
Funders: Österreichischen Akademie der Wissenschaften
Max-Planck-Gesellschaft
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: novelty detection, attention, neural mechanisms, synaptic plasticity, artificial neural networks, cellular mechanisms, memory formation
MeSH terms: Animals, Brain, Brain Mapping, Humans, Memory, Models, Neurological, Neuronal Plasticity, Primates, Rodentia, Synapses

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Neural mechanisms for detecting and remembering novel events

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks